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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7072335inversion1nstd229human GRCh38 chr16: 56,945,057-56,945,142 , GRCh37.p13 chr16: 56,978,969-56,979,054 HERPUD1
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv6987385copy number variation1nstd229human GRCh38 chr16: 56,943,994-56,944,522 , GRCh37.p13 chr16: 56,977,906-56,978,434 HERPUD1
    nsv6981826copy number variation1nstd229human GRCh38 chr16: 56,931,704-56,931,738 , GRCh37.p13 chr16: 56,965,616-56,965,650 HERPUD1
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6497878copy number variation1nstd223human GRCh38 chr16: 56,735,415-57,030,364 , GRCh37.p13 chr16: 56,769,327-57,064,276 HERPUD1, CETP, 7 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6250316mobile element insertion1nstd215human GRCh38 chr16: 56,943,869-56,943,869 , GRCh37.p13 chr16: 56,977,781-56,977,781 HERPUD1
    nsv6250315mobile element insertion1nstd215human GRCh38 chr16: 56,941,773-56,941,773 , GRCh37.p13 chr16: 56,975,685-56,975,685 HERPUD1
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5723068mobile element insertion2nstd211human GRCh38 chr16: 56,935,938-56,935,938 , GRCh37.p13 chr16: 56,969,850-56,969,850 HERPUD1
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5266666copy number variation1nstd204human GRCh38.p13 chr16: 56,927,237-56,943,736 , GRCh37.p13 chr16: 56,961,149-56,977,648 HERPUD1
    nsv5263209copy number variation1nstd204human GRCh38.p13 chr16: 56,771,401-57,423,100 , GRCh37.p13 chr16: 56,805,313-57,457,012 , NUP93, 19 more genes
    nsv5197042mobile element insertion1nstd203human GRCh38 chr16: 56,935,938-56,935,938 , GRCh37.p13 chr16: 56,969,850-56,969,850 HERPUD1
    nsv5150827mobile element insertion1nstd203human GRCh38 chr16: 56,941,151-56,941,165 , GRCh37.p13 chr16: 56,975,063-56,975,077 HERPUD1
    nsv4864167copy number variation1nstd200human GRCh37 chr16: 56,805,348-57,545,260 , GRCh38.p12 chr16: 56,771,436-57,511,348 , POLR2C, 24 more genes
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